Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Yoko Tomiyasu"'
Autor:
Saeko Yokotsuka-Ishida, Mio Nagai, Masayuki Nakamura, Yoko Tomiyasu, Takehiro Hayashi, Yuko Kato, Natsuki Sasaki, Akiyuki Tomiyasu, Hiromi Umehara, Akira Sano, Shu-ichi Ueno
Publikováno v:
Journal of human genetics. 66(6)
The importance of epigenetic control in the development of the central nervous system has recently been attracting attention. Methylation patterns of lysine 4 and lysine 36 in histone H3 (H3K4 and H3K36) in the central nervous system are highly conse
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eca6782d1bd81e3605906ceeeea23a31
https://pubmed.ncbi.nlm.nih.gov/33402700
https://pubmed.ncbi.nlm.nih.gov/33402700
Autor:
Yoko Tomiyasu
Publikováno v:
Bookbird: A Journal of International Children's Literature. 57:43-43
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::277d682471741528ec925683a7a193a9
https://doi.org/10.1353/bkb.2019.0113
https://doi.org/10.1353/bkb.2019.0113
Autor:
Nari Shiokawa, Yoko Tomiyasu, Masayuki Nakamura, Mieko Matsuda, Fujio Umehara, Takehiro Hayashi, Kimiyoshi Arimura, Satsuki Mori, Takanori Ishizuka, Mio Ichiba, Yukie Inamori, Akira Sano, Yuji Okamoto, Yoshiaki Nakabeppu, Akiyuki Tomiyasu, Maiko Kato, Hirochika Shimo
Publikováno v:
Psychiatry and Clinical Neurosciences. 65:105-108
Metachromatic leukodystrophy (MLD) is an autosomal recessive lysosomal storage disease caused by a deficiency of arylsulfatase A. MLD is a heterogeneous disease with variable age at onset and variable clinical features. We evaluated a 33-year-old fem
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::74c1215ad4cb912d7de0a700971df9ba
https://doi.org/10.1111/j.1440-1819.2010.02169.x
https://doi.org/10.1111/j.1440-1819.2010.02169.x
Autor:
Takehiro, Hayashi, Masayuki, Nakamura, Mio, Ichiba, Mieko, Matsuda, Maiko, Kato, Nari, Shiokawa, Hirochika, Shimo, Akiyuki, Tomiyasu, Satsuki, Mori, Yoko, Tomiyasu, Takanori, Ishizuka, Yukie, Inamori, Yuji, Okamoto, Fujio, Umehara, Kimiyoshi, Arimura, Yoshiaki, Nakabeppu, Akira, Sano
Publikováno v:
Psychiatry and clinical neurosciences. 65(1)
Metachromatic leukodystrophy (MLD) is an autosomal recessive lysosomal storage disease caused by a deficiency of arylsulfatase A. MLD is a heterogeneous disease with variable age at onset and variable clinical features. We evaluated a 33-year-old fem
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::9becf1b348bc96c85b6e75bafda9c58e
https://pubmed.ncbi.nlm.nih.gov/21265945
https://pubmed.ncbi.nlm.nih.gov/21265945